Method and system for removal and replacement of lens material from the lens of an eye
There is provided a system, apparatus and methods for developing laser systems that can create a precise predetermined capsulotomy. The systems, apparatus and methods further provide laser systems that reduce the patient-to-patient variability and doctor-to-doctor variability associated with hand held apparatus for performing capsulorhexis and capsulotomies. There is further provided a precise predetermined shot pattern and shaped capsulotomy that is based at least in part on the shape of an IOL and in particular an accommodating IOL.
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This application claims the benefit of priority of provisional application Ser. No. 61/135,950 filed Jul. 25, 2008, the disclosure of which is incorporated herein by reference.
BACKGROUND OF THE INVENTIONThe present invention relates to methods and systems for applying a laser to the natural human crystalline lens to address cataracts, opacifications in the lens, clear lens extraction, removal of natural lens material, use of lens replacement materials and combinations of these. The present invention further relates to methods for determining the shape and position of the natural human crystalline lens and cornea relative to a laser device so as to provide an enhanced method and system for applying a laser to the lens and cornea. The present invention additionally relates to systems and methods that provide predetermined, precise and reproducible laser shot patterns for creating a capsulotomy having a predetermined and precise shape that is reproducible from patient to patient and surgeon to surgeon.
In general, presbyopia is the loss of accommodative amplitude. In generally, cataracts are areas of opacification of the ocular lens which are sufficient to interfere with vision. Other conditions, for which the present invention is directed, include but are not limited to the opacification of the ocular lens.
Presbyopia most often presents as a near vision deficiency, the inability to read small print, especially in dim lighting after about 40-45 years of age. Presbyopia, or the loss of accommodative amplitude with age, relates to the eyes inability to change the shape of the natural crystalline lens, which allows a person to change focus between far and near, and occurs in essentially 100% of the population. Accommodative amplitude has been shown to decline with age steadily through the fifth decade of life.
Cataracts, or the condition when the natural crystalline lens becomes opaque and clouds vision, occurs in millions of people per year and are treated effectively with surgical techniques, such as ultrasonic phacoemulsification pioneered by Kelman 30 years ago. Although the techniques have been refined over the years, safety concerns from ocular trauma, especially to the corneal endothelium from the ultrasonic energy required to break up a hardened cataract is undesirable; especially for those with a compromised corneal endothelium, such as those with Fuchs Dystrophy. Moreover, the use of lasers in the treatment of cataracts has a further issue. Cataracts scatter light, including laser light, and thus, can prevent a laser treatment beam from having the desired tissue effect. Moreover, the light scattering effect of cataracts and other opacifications can make optically determining the position and shape of the lens difficult. Accordingly, as provided in detail in this specification herein improvements in the determination of the lens position and shape, as well as, in the delivery of lasers to lens tissues including the lens capsule, cataractous and opacified tissues are provided.
The established treatment for cataracts is the removal of the opacified human crystalline lens and its replacement with an IOL. In general, IOLs consist of a small plastic lens with plastic side struts, called haptics, to hold the lens in place within the capsular bag inside the eye. Exemplary types of IOLs include monofocal lenses, multifocal IOLs which provide the patient with multiple-focused vision at far and reading distance, and accommodative IOLs which provide the patient with visual accommodation. The flexible nature of many IOLs enables them to be rolled and/or folded up for insertion into the capsule. Examples of IOL are found in U.S. Pat. Nos. 7,188,949, 6,849,091, 5,699,142 and 5,607,472, the disclosures of which are incorporated herein by reference. Commercially available IOLs that, by way of example, may benefit from the present invention are CRYSTALENS and ACRYSOF RESTOR.
A schematic representation of the shape and general structure of an example of an accommodating IOL, along the lines of a CRYSTALENS, is provided in
The CRYSTALENS IOL was developed by Eyeonics and is presently provided by Bausch & Lomb. It is at least in part believed to be disclosed in U.S. Pat. No. 6,849,091. Further information regarding its structure and efficacy is provided by Food and Drug Administration (FDA) PMA P030002 and related documents to that PMA file. The FDA approved indicated use for CRYSTALENS was in part: “The Crystalens™ Model AT-45 Accommodating IOL is intended for primary implantation in the capsular bar of the eye for visual correction of apkakia in adult patients in whom a cataractous lens has been removed and is intended to provide near, intermediate, and distance vision without spectacles. The Crystalens™ IOL provides approximately one diopter of monocular accommodation.” (Nov. 14, 2003 PMA P030002 at Part 2, Summary of Safety and Effectiveness Data, ¶ INDICATIONS FOR USE).
Thus, the CRYSTALENS is an example of an FDA approved accommodating IOL. The term “FDA approved accommodating IOL” refers to any IOL that has obtained FDA approval having an indicated use that provides for accommodation, regardless whether such IOL is actually being employed for such an approved use.
The ACRYSOF RESTOR IOL is provided by Alcon. It is at least in part believed to be disclosed in U.S. Pat. No. 5,669,142. Further information regarding its structure and efficacy is provided by FDA PMA P040020 and related documents to that PMA file. The FDA approved use for RESTOR was in part: “AcrySOF® ReSTOR® IOLs are indicated for the visual correction of aphakia secondary to removal of a cataractous lens in adult patients with and without presbyopia, who desire near, intermediate and distance vision with increased spectacle independence. The lens is intended to be placed in the capsular bag.” (Apr. 24, 2004, PMA P040020, at Part 2, Summary of Safety and Effectiveness Data, ¶ INDICATIONS).
Thus, the RESTOR is an example of an FDA approved IOL for near, intermediate and distance vision. The term “FDA approved IOL for near, intermediate and distance vision” refers to any IOL that has obtained FDA approval having an indicated use that provides for near, intermediate and distance vision, regardless whether such IOL is actually being employed for such an approved use. The CRYSTALENS would also be an example of an FDA approved IOL for near, intermediate and distance vision. Moreover, the RESTOR and CRYSTALENS are examples of FDA approved IOLs that reduce and/or eliminate the need for spectacles.
The removal of the opacified natural crystalline lens and replacement with a lens replacement material, such as an FDA approved IOL, presently employs a capsulorhexis and/or a capsulotomy procedure. A capsulorhexis generally consists of the removal of a part of the anterior lens capsule and the creation of a hole or opening in the lens capsule, that results from at least in part a tearing action. A capsulotomy generally consists of a cutting of the lens capsule, without or with minimum tearing of the capsule. Thus, to remove the opacified natural lens material, the lens capsule is opened. There are several known techniques for performing a capsulorhexis and a capsulotomy.
One of these capsulorhexis techniques is a can opener approach. This approach uses a small bent needle to make small incisions around the anterior lens capsule to create an opening in the lens through which the lens could be removed. This technique quite often results in the opening in the lens capsule having ragged edges. Another of these techniques is a Continuous Curvilinear Capsulorhexis (CCC). CCC uses the same type of bent needle to begin the tear in the anterior lens capsule and then uses this needle and/or special forceps which are manually pulled to create a generally circular hole in the lens capsule. CCC, in comparison to the can opener approach, reduces the ragged edge around the opening in the lens that occurred with using the can opener technique. However CCC does not eliminate the formation of these ragged edges and there presence is dependent upon surgical skill and technique.
The use of a Fugo plasma blade to create the hole in the anterior capsule may also be used. This technique is referred to as a capsulotomy. The Fugo plasma blade is a hand held device and was originally utilized in dentistry. It is an electro magnetic device that focuses its energy on a blunt cutting filament. Information regarding the Fugo plasma blade can be found in FDA PMA K063468, K001498, K041019, and K050933.
To date is it believed that all prior techniques and apparatus and in particular all prior FDA approved apparatus for creating an opening in the anterior capsule of the lens, have to varying degrees given rise to irregular shapes, ragged edges, jagged edges, or tags in or along the edge of the opening, and/or combinations of these edge features. Moreover, it is believed that all of these prior techniques and apparatus, which are performed by hand, in general can only produce cuts or holes in the shape of a circle or an ellipse, i.e., they can only be used to provide geometric shapes and cannot be used to provide non-geometric shaped cuts. Further, because these are hand held devices the shape of these cuts varies from patient to patient and surgeon to surgeon. Thus, it is not believed that these hand held devices and non-automated techniques can provide the precise predetermined capsulotomy of the present invention.
The presence of the above described edge features, the inability to create precise predetermined and reproducible shaped cuts and the variability associated with prior techniques and apparatus for performing capsulotomies and capsulorhexises are individually and collectively undesirable and can present difficulties and problems, especially with the use of accommodative IOLs. Furthermore, the limited number of shapes for capsulotomies and capsulorhexis and the variability associated with these prior techniques is believed to be an impediment to the development of new accommodative IOLs. It is further believed that this limited number of shapes and variability is an impediment to the amount of accommodation that can be obtained from presently known IOLs and the instances where little to no accommodation is realized by the patient.
SUMMARYIt is desirable to develop systems that would reduce or eliminate these undesirable edge features, provide greater control in the creation of the opening in the lens capsule and make these improvements patient and surgeon independent, or at least, reduce the variability from patient to patient and surgeon to surgeon, associated with the formation of these undesirable features that is found with the use of present techniques and tools.
The present invention, among other things, solves this need by providing greater control in the creation of opening in the lens, in particular the creation and position of the edge of the hole, and the ability to reduce the occurrence of undesirable edge features, and do so in a manner that is less surgeon and patient dependent. Thus, there is provided herein a system and method to perform precise predetermined capsulotomies.
The novel and improved methods and systems for the performance of a capsulotomy and for measuring and determining lens position and shape, which comprise aspects of the present inventions and which are set forth in detail in the present patent specification, may provide for better implementation of other methods and systems for delivering laser beams to the lens of the eye, such as those disclosed in published applications US 2007/17379A1, US 2007/173795A1, US2007/185475A1, WO 2007/084694 A2 (now U.S. Ser. No. 12/217,295), WO 2007/084627A2 (now U.S. Ser. No. 12/217,285), the disclosures of which are incorporated herein by reference.
Provided herein are embodiments of the present invention. There is provided a system and a method of making a system for reducing eye to eye and surgeon to surgeon variability in performing procedures to create cuts in the capsule of the lens of the eye. This system comprising a therapeutic laser for producing a therapeutic laser beam, an optical path for directing the therapeutic laser beam from the therapeutic laser to the lens of the eye, and, a control system for at least directing the therapeutic laser beam in a predetermined non-geometric shaped shot pattern on a portion of the anterior capsule of the lens of the eye to create a precise predetermined non-geometric shaped capsulotomy. This system may further include a shot pattern wherein the predetermined shot pattern comprises at least one essentially straight section, wherein the predetermined shot pattern comprises at least two essentially straight sections, wherein the predetermined shot pattern comprises a first essentially straight section, a second essentially straight section, a first curved section and a second curved section, or wherein the predetermined shot pattern comprises a first essentially straight section, a second essentially straight section, a first curved section and a second curved section; and, the first essentially straight section is connected to the second and third curved sections.
There is also provided system and a method of making such system comprising a therapeutic laser for producing a therapeutic laser beam, an optical path for directing the therapeutic laser beam from the therapeutic laser to the lens of the eye, and, a control system for at least directing the therapeutic laser beam in a predetermined non-geometric shaped shot pattern on a portion of the anterior capsule of the lens of the eye to create a precise predetermined non-geometric shaped capsulotomy and having a means for determining the apex of the lens of the eye.
There is further provided a system for reducing eye to eye and surgeon to surgeon variability in performing procedures to create cuts in the capsule of the lens of the eye having a therapeutic laser for producing a therapeutic laser beam, an optical path for directing the therapeutic laser beam from the therapeutic laser to the lens of the eye, a control system for at least directing the therapeutic laser beam in a predetermined non-geometric shaped shot pattern on a portion of the anterior capsule of the lens of the eye to create a precise predetermined non-geometric shaped capsulotomy, and the shot pattern shape being based at least in part on the shape of an IOL.
There is yet further provided shot patterns for the delivery of the laser to the lens of the eye that are based upon shape of an IOL wherein the IOL is an FDA approved accommodating IOL, wherein the IOL is an FDA approved IOL for near, intermediate and distance vision, wherein the IOL is an FDA approved IOL that reduces or eliminates the need for spectacles.
There is additionally provided a system for reducing eye to eye and surgeon to surgeon variability in performing procedures to create cuts in the capsule of the lens of the eye, the system comprising, a therapeutic laser for producing a therapeutic laser beam, an optical path for directing the therapeutic laser beam from the therapeutic laser to the lens of the eye, a control system for at least directing the therapeutic laser beam in a predetermined non-geometric shaped shot pattern on a portion of the anterior capsule of the lens of the eye to create a precise predetermined non-geometric shaped capsulotomy, the shot pattern shape being based at least in part on the shape of an IOL, the IOL having at least one hinge, and the shot pattern essentially following the shape of the IOL.
There is still further provided a system for reducing eye to eye and surgeon to surgeon variability in performing procedures to create cuts in the capsule of the lens of the eye, comprising a control system for at least directing the therapeutic laser beam in a shot pattern on a portion of the anterior capsule of the lens of the eye to create a cut in the capsule, the shot pattern having an X, Y and Z direction component, the delivery of the shots in the shot pattern relative to the X, Y and Z directional components being delivered in a jigsaw cut, having a Z direction sweep, and wherein the Z direction sweep is of a magnitude that it substantially reduces the number of missed cuts which reduces eye to eye and surgeon to surgeon variability.
There is also provided a method for making a laser device for creating a precise predetermined capsulotomy, said method comprising obtaining a laser device having a therapeutic laser, analyzing an IOL to obtain information about the IOL, developing a non-geometric shaped shot pattern for the delivery of the therapeutic laser to the capsule of the lens of the eye, said development being based at least in part upon the information obtained from said analysis, and, providing the non-geometric shot pattern to said laser device. By way of example such providing can be accomplished by supply or downloading a program to the laser controller containing the information regarding the shot pattern.
One of ordinary skill in the art will recognize, based on the teachings set forth in these specifications and drawings, that there are various embodiments and implementations of these teachings to practice the present invention. Accordingly, the embodiments in this summary are not meant to limit these teachings in any way.
In general, the present inventions relates to methods and systems for providing a laser to the natural human crystalline lens to address cataracts, opacifications in the lens, clear lens extraction, removal of natural lens material, replacement of that material with replacement material, and combinations of these. The present invention further relates to methods for determining the shape and position of the lens so as to provide an enhanced method and system for providing a laser to the natural human crystalline lens for addressing these conditions.
The present invention provides a system and method for determining the location, shape and apex of the lens and cornea with respect to the laser device or system and for the use of this determination in performing a capsulotomy and in performing the removal of the clear, opacified, or cataractous lens material of a natural crystalline lens. Thus, in general a laser system, i.e., a laser device, for treating patients is provided as shown by way of example in
In general, the treatment laser 101 should provide a beam 104 that is of a wavelength that transmits through the cornea, aqueous and lens. The beam should be of a short pulse width, together with the energy and beam size, to produce photodisruption. Thus, as used herein, the term laser shot or shot refers to a laser beam pulse delivered to a location that results in photodisruption. As used herein, the term photodisruption essentially refers to the conversion of matter to a gas by the laser. In particular, wavelengths of about 300 nm to 2000 nm may be employed. Pulse widths from about 1 femtosecond to 100 picoseconds may be employed. Energies from about a 1 nanojoule to 1 millijoule may be employed. The pulse rate (also referred to as pulse repetition frequency (PRF) and pulses per second measured in Hertz) may be from about 1 KHz to several GHz. Generally, lower pulse rates correspond to higher pulse energy in commercial laser devices. A wide variety of laser types may be used to cause photodisruption of ocular tissues, dependent upon pulse width and energy density. Thus, examples of such lasers are disclosed in 2007/084694 A2 and WO 2007/084627A2, which are incorporated herein by reference. These and other similar lasers may be used a therapeutic lasers.
In general, the optics for delivering 102 the laser beam 104 to the natural lens of the eye should be capable of providing a series of shots to the natural lens in a precise and predetermined pattern in the x, y and z dimension. The optics should also provide a predetermined beam spot size to cause photodisruption by the laser pulses delivered to the lens or cornea.
In general, the control system 103 for delivering the laser beam 104 may be any computer, controller, and/or software hardware combination that is capable of selecting and controlling x y z scanning parameters and laser firing. These components may typically be associated at least in part with circuit boards that interface to the x y scanner, the z focusing device and/or the laser. The control system may also, but does not necessarily, have the further capabilities of controlling the other components of the system, as well as, maintaining data, obtaining data and performing calculations. Thus, the control system may contain the programs that direct the laser through one or more laser shot patterns. Similarly, the control system may be capable of processing data from the slit scanned laser 117 and camera 118 and/or from a separate controller for the slit scanned laser system or camera.
The laser optics for delivering 102 the laser beam 104 comprise a beam expander telescope 105, a z focus mechanism 106, a beam combiner 107, an x y scanner 108, and focusing optics 109. There is further provided relay optics 110, camera optics 111, which include a zoom, and a first ccd camera 112.
Optical images 113 of the eye 114 and in particular optical images of the natural lens 115 of the eye 114 are conveyed along a path 113. This path 113 follows the same path as the laser beam 104 from the natural lens 115 through the laser patient interface 116, the focusing optics 109, the x y scanner 108 and the beam combiner 107. There is further provided a laser patient interface 116, and a structured light source 117 and a structured light camera 118, including a lens.
A structured light source 117 may be a slit illumination having focusing and structured light projection optics, such as a Schafter+Kirchhoff Laser Macro Line Generator Model 13LTM+90CM, (Type 13LTM-250S-41+90CM-M60-780-5-Y03-C-6) or a StockerYale Model SNF-501L-660-20-5, which is also referred to as a slit scanned laser. In this embodiment the structured illumination source 117 also includes slit scanning means 119.
When using a scanned slit illumination the operation includes positioning the slit at an acute angle to the crystalloine lens' AP axis and to one side of the lens, taking an image then maintaining the same angle, moving the slit a predetermined distance, then taking another image, and then repeating this sequence until the entire lens is observed through the series of slit sections. The nominal slit angle can be approximately 15 to 30 degrees from the AP axis. Any visible or near IR wavelength source compatible with the camera may be used. Low coherence length sources are preferable to reduce speckle noise.
The structured light illumination source 117 and the structured light camera 118 are arranged in an angled relationship. The angled relationship may be but is not required to be in the so-called Scheimpflug configuration, which is well-known. The structured light source 117, in conjunction with the slit scanning means 119, projects a line and or a plurality of lines onto the eye lens 115 at an angle or plurality of angles. The light scattered at the eye lens 115 forms the object to be imaged by the lens 247 and focused onto the camera system 118. Since the slit illuminated image in the eye lens 115 may be at a large angle with respect to the camera 118, this presents a large depth of field to the camera and the entire slit image may not be in sharp focus at the camera. By tilting the camera at an angle or plurality of angles the image along the illuminated plane can be in sharper focus. To the extent that a shaper focus is not obtained, arithmetic data evaluation means are further provided herein to determine a more precise location of the illuminated structures with respect to the laser device.
The images from the camera 118 may be conveyed to the controller 103 for processing and further use in the operation of the system. They may also be sent to a separate processor and/or controller, which in turn communicates with the controller 103. The structured light source 117, the camera 118 and the slit scanning means 119 comprise a means for determining the position, shape and apex of the lens and cornea in relation to the laser system. Alternate means of measuring the position, shape and apex of the lens and cornea may be used in lieu of the specific embodiment described herein. Other equivalent biometric methods for measuring the lens and cornea include rotating Scheimpflug configurations such are used in the commercial PENTACAM OCULUS device, optical coherence tomography (OCT) and B-scan ultrasound technologies.
In general, the present invention provides for the delivery of the laser beam in patterns that utilize, or are based at least in part on, lens geometry, curvature of the lens and/or the position and location of the lens and cornea with respect to various apparatus. More specifically, the invention could utilize measurements of the radii or curvature, center of curvature and apex of the lens and cornea to control the position and orientation of the capsulotomy and the position and shape of the envelope of cuts in the lens nucleus used to fragment the lens for removal. As part of the present invention the concept of matching and/or compensating for the curvature and position of the capsule of the lens is provided. Anterior and posterior lens curvatures and lens location measurements can be used in the context of Kuszak aged lens models, Burd's eye model, Burd et al. Vision Research 42 (2002) 2235-2251, or on specific lens measurements to determine the position of the capsulotomy and shape of the envelope defining the boundary of cuts within the lens fibrous mass. Thus, in general, these laser delivery patterns are based in whole and/or in part on the mathematical modeling and actual observation data regarding the shape of the lens, the position of the lens and/or the geometry of the lens.
The delivery of laser shot patterns for the removal of lens material is provided. Three primary activities are provided herein. The first activity involves the anterior surface of the lens capsule. The second activity involves the lens material that is contained within the capsule, i.e., the interior structures of the lens, such as the cortex and the nucleus and cataractous material contained therein. The third activity involves the use of a lens replacement material, including but not limited to IOLs, within the lens capsule after interior structures of the lens have been removed.
Thus, there are provided novel methods and systems for producing cuts, i.e., incisions in the anterior lens capsule. These cuts are created by the therapeutic laser beam 104 being delivered to the anterior lens capsule in precise predetermined and highly reproducible patterns, delivery results in precise predetermined and highly reproducible shaped cuts in patterns as described and taught herein, or as may be called for by the use of a particular IOL or other device or material to be inserted within the lens capsule. As used herein geometric shaped patterns or cuts refers to circular and elliptical shaped patterns or cuts. As used herein non-geometric shaped patterns or cuts refers to all other shapes that are not circular or elliptical.
The methods and systems to create these cuts in the anterior capsule provide superior results to the handheld methods and apparatus previously known for performing capsulorhexus and capsulotomy, and thus, the methods and systems disclosed herein are considered to be a substantial advancement in these techniques. In addition the delivery of the laser beam shots in a manner that greatly reduces the risk of a missed cut, which depending upon the particular application may be very significant is provided. Moreover, as provided in the following examples, anterior capsule cuts are envisioned and provided that may be a continuous cuts, cuts and lands (uncut capsule portions between cuts) and perforations. Thus, as used herein the terms “missed cut” or “missed cuts” refer to a cut that was intended to be carried out by the delivery of a particular laser shot pattern, but which did not occur because the laser beam missed the lens capsule or targeted lens material. Thus, in a cut and land pattern the lands would not be considered missed cuts, if they were intended to be left uncut by the laser pattern.
The cuts in the lens anterior surface are for the purpose of creating an opening in the lens capsule for the removal of the interior structures of the lens. To facilitate this removal there are provided various laser shot patterns that cut the interior structure of the lens into small volumes, which volumes can then be removed from the lens capsule. These small volumes can range from about 0.064 mm3 to about 8 mm3. Thus a grid laser shot pattern within the interior structures of the lens, which creates cube shaped volumes of interior lens material, can be employed. These cubes can range in size from a side having a length of about 0.4 mm to about 2 mm with the characteristic dimension of the cube chosen in part to match the internal diameter of the tip of aspiration probe to be used to remove the lens tissue. Additionally, this invention is not limited to the formation of cubes and other volumetric shapes of similar general size may be employed. For example arrangement of other shapes such as triangles and pie sliced volumes may be employed.
The laser cut in the anterior capsule is used to create a small opening in the lens anterior surface of the lens capsule for removal of the sectioned volumes of interior material. Thus, this procedure may be used to treat cataracts. This procedure may also be used to remove a lens having opacification that has not progressed to the point of being cataractous. This procedure may further be used to remove a natural lens that is clear, but which has lost its ability to accommodate. In all of the above scenarios, it being understood that upon removal of the lens material the lens capsule would subsequently house a suitable replacement, such as an IOL, accommodative IOL, or synthetic lens refilling materials. Moreover, the size and the shape of the opening is variable and precisely controlled and preferably for presently known lens refilling materials and IOLs is 2 mm or less diameter for lens refilling applications and about 5 mm for IOLs.
The order in which these activities are performed may depend upon the particular characteristics of the internal lens structure, the density of the cataract, the position of the cataract, the type of device used to remove the internal lens material once it has been sectioned into small volumes, the type and power of the laser used, the amount and size of gas bubbles that are produced by the laser, and other factors. Thus, although the examples herein provide for an order of performing the activity of cutting the anterior surface of the lens and sectioning the interior structures of the lens, it should be recognized that this order can be changed, as well as performed essentially simultaneously.
The laser system for treating patients of the present invention is capable of making precise and predetermined cuts in the capsule of the lens thus giving rise to capsulotomies that are of precise and predetermined shapes. Thus, there is provided the method of obtaining and analyzing the shape and structure of an IOL, and in particular obtaining and analyzing the shape and structure of an accommodating IOL, an IOL that reduces and/or eliminates the need for spectacles, and/or an IOL for near, intermediate and distance vision, including but limited to FDA approved versions of said IOLs. Based upon this analysis an optimized shape and position for the capsulotomy for use with a particular IOL, or grouping of similarly shaped IOLs, is determined. A predetermined shot pattern for making this optimized shaped capsulotomy is then provided to the laser system, preferably by providing the shot pattern to the control system 103. The laser system can then be used for one or all of the following procedures, determining the shape and position of the anterior surface of the lens, and in particular the anterior surface of the lens capsule, determining the apex of the lens capsule in relation to the laser system, performing a laser capsulotomy having the precise and predetermined shape selected for a particular type of IOL, and removal of the natural lens material.
Thus, for example, the shape of a precise capsulotomy and its corresponding shot pattern may consist of essentially straight sides, which each side being connected by curved or rounded sections. An example of this type of predetermined cut is illustrated in
The precise and predetermined shot pattern, opening, capsulotomy and cut may have only a single straight section or it may have two, three, four, five, or more. Moreover, in addition to essentially straight sections, there may be sections in which the radius of curvature is substantially reduced in comparison to other sections of the pattern, opening, capsulotomy or cut. Thus, for example, as shown in
Thus, there is provided techniques, systems and apparatus to deliver laser beam in a shot pattern to the lens of the eye and in particular to the capsule of the lens of the eye in a precise and predetermined manner to provided for a precise predetermined capsulotomy. The shape of these patterns may be delivered using either the jigsaw or ring delivery sequences provided herein.
When performing laser assisted cataract surgery the process of cutting the nucleus with a photodisruption laser can cause a buildup of gas bubbles sufficiently near the soft cortex to allow the gas bubbles to propagate toward the capsule. In those situations where bubbles collect in close proximity to the anterior capsule, when the laser attempts to cut the capsulotomy, the sudden release of bubbles may change the position of the anterior capsule during the delivery of the laser shot pattern causing the laser to miss the capsule resulting in missed cuts, at least partially around the circumference of the capsulotomy. To solve this problem, there is provided herein a special cutting pattern that is less dependent of capsule position versus time and provides cutting of the capsule despite position changes of the capsule during the laser capsulotomy procedure. Thus, resulting in substantially reduced or no missed cuts.
There is provided herein the use of laser shot patterns having a large range of Z swept at a high rate of speed, while the XY position is moved in a circular, or elliptical or other pattern or desired shape, more slowly so that the laser cutting action occurs multiple times over essentially the same XY position. Thus, it could be envisioned that the laser beam is operating like the tip of a jigsaw blade moving up and down rapidly compared to the XY positioning to create the cut shape. In this way, if the anterior capsule shifts during the cut, due to gas bubble propagation or any other reason, the cut will still be made to the capsule, albeit perhaps outside the center region of the z direction up-down distribution of shots, and more to the anterior or posterior ends of that distribution. For laser cutting of the nucleus where a great deal of bubble buildup is created, a Z range, or up-down range of the cut should be approximately 1 mm in extent, nominally centered on the anterior capsule which would allow approximately ±475 μm of capsule movement and still provide cutting of a 25 μm thick capsule.
In addition to enabling cutting of a capsule that moves move during the procedure, this procedure can be used to compensate for static errors in capsule position due to for example measurement errors. In this way the extent of the Z range may be increased by the known error of the system.
In addition to the large Z range sweeps disclosed herein, there is also contemplated the use of a smaller Z range of cut motion for the case where the uncertainty in capsule position from both static measurement error and anticipated change in position might be smaller, perhaps in the range of hundreds of μm or in the case of highly precise measurement data and near zero movement of the capsule during surgery. In such a case the Z range could be tens of μm—enough range to cut through the capsule thickness.
The Z range sweep in the capsulotomy shot pattern provides for the ability to optimize laser surgery efficiency in cataract removal procedures. Thus, the nucleus of the lens can be sectioned into small volumes before the capsulotomy is performed. In this way any gas bubbles that are formed by the sectioning of the nucleus will be trapped within the capsule. By keeping the gas bubbles inside of the capsule, their effect on laser delivery is reduced, when compared to their effect if they escape from the capsule and migrate into the aqueous or collect and build up next to the posterior of the cornea. The detrimental effect of shooting the laser beam through a bubble increases as the distance that the beam has to travel after passing through the bubble before reaching its intended point increases. Thus, by trapping the bubble in the capsule this distance is keep to an absolute minimum and thus the detrimental effect of shooting through the bubbles is similarly minimized.
The accumulation of bubbles within the capsule, however, increases the likelihood that the lens and/or capsule will shift during the capsulotomy as the bubbles escape through the cuts in the lens capsule. As noted above this shifting could result in missed cuts and an incomplete capsulotomy. Thus, the Z range sweep avoids any missed cuts from lens or capsule movement and accordingly provides the synergistic advantages of increased laser efficiency, reduced detrimental effect of gas bubbles, and reduced missed cuts in the capsulotomy.
Thus there is provided a system and method to optimize laser surgery efficiency in an embodiment of the invention by allowing the nucleus to be cut first, and the gas bubbles formed from such cutting contained within the capsule, until the capsulotomy is performed. The containing of the gas bubbles within the capsule avoids having to shoot through bubbles in the anterior chamber caused but creating the capsulotomy first. This solution, however, can lead to the accumulation of bubbles inside the fibrous mass of the lens which may cause the capsule to move during capsulotomy. To address this potential movement the invention further provides for the varying z direction movement of the laser beam. However, it is also understood that, one case where the uncertainty of capsule movement is small is the case where the capsulotomy is laser cut prior to the cutting of the nucleus material and no bubbles have been placed in the lens. In this case if the uncertainty in position is sufficiently small that the extent of the z range is sufficiently small, that only a superficial amount of bubbles may be present in the anterior chamber which may not interfere with laser cutting of the nucleus. It should further be understood that when referring to a sequence of cutting structures, such as described in this paragraph, that a step the order of sequence is defined by when a substantial majority of the cuts are performed in the one structure before another structure, i.e., the placement of a few laser shots in an other structures during delivery of the shot pattern to the first structure will not prevent the first structure from being considered the first structure in the sequence.
A further embodiment of the present systems and methods is to define a high accuracy position measurement of the anterior capsule, so as to provide in general greater accuracy, precisions and reproducibility from patient to patient for the capsulotomy. Thus, there is provided a method applying slit technology with new and innovative methods to determine the apex of the lens of the eye, with respect to the therapeutic laser device, and thus, providing accurate measurements and relative position determinations for performing procedures on the lens of the eye.
Thus, turning to
In
In
In general the RANSAC algorithm as employed herein is based upon a number of algorithm parameters that are chosen to keep the level of probability of convergence of the fit to the circle fit parameters reasonably high. The approach is iterative wherein each iteration is used to refine the selection of which pixels (inliers) are best used to determine the parameters of the fit circle and which should be excluded (outliers) and to, at the same time refine the best fit parameters based on the pixels selected in the latest iteration. Thus, a model was fitted to the initial hypothetical inliers, to make an initial estimate of the parameters of the fit circle, i.e. shape and position of the lens from observed data. Based on the initial parameter estimates, all other data points, pixels, are checked to see how far they fall from the fitted model and the set of inliers and outliers is adjusted. The model was then re-estimated from all adjusted inliers. The model is evaluated by estimating a parameter related to the total magnitude of error of the inliers relative to the model. This procedure was repeated, and the precision of the estimate is refined at each iteration
An example of a RANSAC algorithm is as follows:
The series of best fit parameters for circles estimated for different slit beam locations is then used in a least squares algorithm to determine the radius of curvature and center of curvature of the anterior capsule, assuming that a sphere is a good representation of the shape of the capsule in the central region of interest.
Thus, by photographing the light scattered by lens structures from a laser slit beam positioned sequentially to a series of different slit locations and applying a RANSAC algorithm and/or a RANSAC algorithm and a least squares non-liner regression with a sphere fit, to the data obtained from each of those series of illuminations, a detained image of the shape and position of the lens relative to the laser device can be obtained. In the current embodiment, the shape and position of the anterior lens capsule is characterized by the estimation of the radius and center of curvature. Using this information, the position of the apex of the lens relative to the laser device, and in particular the therapeutic laser, can be determined for use in positioning and orienting the capsulotomy. Though not shown here, an exactly analogous method as described above for the anterior lens capsule can be used to determine the center and radius curvature of the anterior cornea. Since the center of curvature of the lens and cornea are known in most cases to fall close to the visual axis of the eye, these two points define a line which intersects the anterior lens capsule at or near the visual axis and position of the intersection can be used to center the capsulotomy cut at or near the visual axis as is generally desired for best optical outcome.
Having both the shape, position and apex of the lens provides the ability to greatly increase the accuracy and reproducibility of the capsulotomy. Determining the apex and shape of the lens relative to the laser device enables the use of a shot pattern for the capsulotomy that minimizes the number of shots that must be anterior to the anterior lens capsule to make certain that the capsulotomy is completed and the capsule portion can be readily removed. Thus, referring for example to
A further optimization of the method and system to enhance flexibility regarding the aspiration of lens material from the lens capsule is provided. In sectioning the lens material it is possible that the some of the cut fragments of the fibrous mass may escape the capsular bag, either by floating or because of gas bubbles or just naturally, unless means of preventing such escape are provided. Therefore another aspect of the present method and system is to provide a means to restrain these fragments until they are ready to be aspirated out. Such a means is provided by performing only a partial cut of the capsule, leaving the capsule flap attached to serve as a restraint preventing and/or reducing the escape of sectioned lens material. Once aspiration is called for the partial cut to the capsule can be completed, i.e., the capsulotomy is completed, and the section lens material aspirated out of the lens capsule.
In all of the laser shot patterns provided herein it is preferred that the laser shot patterns generally follow the shape of the lens and placement of individual shots with respect to adjacent shots in the pattern are sufficiently close enough to each other, such that when the pattern is complete a sufficiently continuous layer and/or line and/or volume of lens material has been removed. Shot spacing of lesser or greater distances are contemplated herein and including overlap as necessary to obtain the desired results. Shot spacing considerations include gas bubble dissipation, volume removal efficiency, sequencing efficiency, scanner performance, and cleaving efficiency among others. For example, by way of illustration, for a 5 μm size spot with an energy sufficient to cause photodisruption, a spacing of 20 μm or greater results in individual gas bubbles, which are not coalesced and dissipate more quickly, than with close shot spaces with the same energy, which result in gas bubble coalescence. As the shot spacing gets closer together volume efficiency increases. As shot spacing gets closer together bubble coalescence also increases. Further, there comes a point where the shot spacing becomes so close that volume efficiency dramatically decreases. For example, by way of illustration, for a 450 femtosecond pulse width and 2 microjoules energy and about a 5 μm spot size with a 10 μm separation results in cleaving of transparent ocular tissue. As used herein, the term cleaving means to substantially separate the tissue. Moreover, the forgoing shot spacing considerations are interrelated to a lesser or greater extent and one of skill in the art will know how to evaluate these conditions based upon the teachings of the present disclosure to accomplish the objectives herein. Finally, it is contemplated that the placement of individual shots with respect to adjacent shots in the pattern may in general be such that they are as close as possible, typically limited by the size and time frame of photodisruption physics, which would include among other things gas bubble expansion of the previous shot. As used herein, the time frame of photodisruptive physics referrers to the effects that take place surrounding photodisruption, such as plasma formation and expansion, shock waive propagation, and gas bubble expansion and contraction. Thus, the timing of sequential pulses such that they are timed faster than some of, elements of, or all of those effects, can increase volumetric removal and/or cleaving efficiency. Accordingly, we propose using pulse repetition frequencies from 5 KHz to 1 MHz., which could be accomplished by a laser with the following parameters: a mode lock laser of cavity length from 3 meters to 3 cm. Such high PRF lasers can more easily produce multiple pulses overlapping a location allowing for a lower energy per pulse to achieve photodisruption.
The terms first, second, third, etc. as used herein are relative terms and must be viewed in the context in which they are used. They do not relate to timing, unless specifically referred to as such. Thus, a first cut may be made after a second cut. In general, it is preferred to fire laser shots in general from posterior points in the laser pattern to anterior points, to avoid and/or minimize the effect of the gas bubbles resulting from prior laser shots. However, because of the varied laser shot patterns that are provided herein, it is not a requirement that a strict posterior to anterior shot sequence be followed. Moreover, in the case of cataracts it may be advantageous to shoot from anterior to posterior, because of the inability of the laser to penetrate substantially beyond the cataract.
Thus, there is provided a method for the structural modification of the lens material to make it easier to remove while potentially increasing the safety of the procedure by reducing and/or eliminating the need to use high frequency ultrasonic energy used in Phaco emulsification. In general, the use of photodissruption cutting in a specific shape patterns is utilized to create sectioned lens material, i.e., to carve up the lens material into sectioned volumetric shapes, such as the tiny cube like structures shown in
As illustrated in
The creation of capsulotomy for the surgeon to access the lens to remove the lens material is illustrated in
Since the lens capsule is approximately 5 to 15 μm thick, it is desirable for the depth of the cut to be typically between 5 and several hundred um, although there is not much penalty for cutting several millimeters. With greater precision regarding the location and shape of the lens and lens apex the thickness of the band and in particular the amount of the band that is above the lens capsule and in the aqueous can be reduced. The shape of the capsulotomy can be elliptical with the x axis different then the y axis or other shapes. Thus, the shape of the capsulotomy can be any shape that provides a benefit for a particular IOL, for example the shape of the capsulotomy can be circular or elliptical geometric shapes or can be, square, rectangular, or other non-geometric shapes. The shape will be based at least in part upon and be determined at least in part by, the aspects of IOLs and in particular accommodating IOLs and IOLs that reduce and/or eliminate the need for spectacles. A particular IOL, such as FDA approved IOLs discussed herein, may benefit from and/or may require a particular capsulotomy shape and opening smoothness.
A jigsaw delivery sequence or pattern for performing a precision capsulotomy is further provided herein. As illustrated in
As illustrated in
The combination of the patterns and types of cuts provided herein can be interchanged and other shapes of patterns and position relative the XY center of the lens may be employed. Moreover, Because there is a greater likelihood for a missed laser shot with the band cut, i.e., the ring delivery sequence or pattern, such as shown in
From the foregoing description, one skilled in the art can readily ascertain the essential characteristics of this invention, and without departing from the spirit and scope thereof, can make various changes and/or modifications of the invention to adapt it to various usages and conditions.
Claims
1. A system for reducing eye to eye and surgeon to surgeon variability in performing procedures to create cuts in the capsule of the crystalline lens of the eye, the system comprising:
- a. a therapeutic laser for producing a therapeutic laser beam;
- b. an optical path for directing the therapeutic laser beam from the therapeutic laser to the lens of the eye; and,
- c. a control system for at least directing the therapeutic laser beam in a predetermined non-geometric shaped shot pattern on a portion of the anterior capsule of the lens of the eye to create a precise predetermined non-geometric shaped capsulotomy, wherein the predetermined shot pattern comprises an essentially straight section.
2. The system of claim 1, wherein the predetermined shot pattern comprises a second essentially straight section.
3. The system of claim 2, wherein the predetermined shot pattern comprises a first curved section and a second curved section.
4. The system of claim 3 wherein: the first essentially straight section is connected to the first and second curved sections.
5. The system of claim 1 comprising a means for determining the apex of the lens of the eye.
6. A system for reducing eye to eye and surgeon to surgeon variability in performing procedures to create cuts in the capsule of the crystalline lens of the eye, the system comprising:
- a. a therapeutic laser for producing a therapeutic laser beam;
- b. an optical path for directing the therapeutic laser beam from the therapeutic laser to the lens of the eye;
- c. a control system for at least directing the therapeutic laser beam in a predetermined non-geometric shaped shot pattern on a portion of the anterior capsule of the lens of the eye to create a precise predetermined non-geometric shaped capsulotomy; and,
- d. the shot pattern shape being based at least in part on the shape of an IOL, wherein the predetermined shot pattern comprises an essentially straight section.
7. The system of claim 6, wherein the predetermined shot pattern comprises a second essentially straight section.
8. The system of claim 7, wherein the predetermined shot pattern comprises a first curved section and a second curved section.
9. The system of claim 8, wherein: the essentially straight section is connected to the first and second curved sections.
10. The system of claim 6 comprising a means for determining the apex of the lens of the eye.
11. The system of claim 6, wherein the IOL is an FDA approved accommodating IOL.
12. The system of claim 6, wherein the IOL is an FDA approved IOL for near, intermediate and distance vision.
13. The system of claim 6, wherein the IOL is an FDA approved IOL that reduces or eliminates the need for spectacles.
14. A system for reducing eye to eye and surgeon to surgeon variability in performing procedures to create cuts in the capsule of the crystalline lens of the eye, the system comprising:
- a. a therapeutic laser for producing a therapeutic laser beam;
- b. an optical path for directing the therapeutic laser beam from the therapeutic laser to the lens of the eye;
- c. a control system for at least directing the therapeutic laser beam in a predetermined non-geometric shaped shot pattern on a portion of the anterior capsule of the lens of the eye to create a precise predetermined non-geometric shaped capsulotomy;
- d. the shot pattern shape being based at least in part on the shape of an IOL, the IOL having at least one hinge; and,
- e. the shot pattern essentially following the shape of the IOL, wherein the shot pattern is positioned on the lens of the eye so that the capsulotomy is in part position outside of the hinge.
15. A system for reducing eye to eye and surgeon to surgeon variability in performing procedures to create cuts in the capsule of the crystalline lens of the eye, the system comprising:
- a. a therapeutic laser for producing a therapeutic laser beam;
- b. an optical path for directing a therapeutic laser beam from the therapeutic laser to the lens of the eye;
- c. a control system for at least directing the therapeutic laser beam in a shot pattern on a portion of the anterior capsule of the lens of the eye to create a cut in the capsule;
- d. the shot pattern having an X, Y and Z direction component;
- e. the delivery of the shots in the shot pattern relative to the X, Y and Z directional components being delivered in a jigsaw cut, having a Z direction sweep; and,
- f. wherein the Z direction sweep is of a magnitude that it substantially reduces the number of missed cuts which reduces eye to eye and surgeon to surgeon variability.
16. A method for making a laser device for creating a precise predetermined capsulotomy, said method comprising:
- a. obtaining a laser device having a therapeutic laser;
- b. analyzing an IOL to obtain information about the IOL;
- c. developing a non-geometric shaped shot pattern for the delivery of the therapeutic laser to the capsule of the crystalline lens of the eye;
- d. said development being based at least in part upon the information obtained from said analysis; and,
- e. providing the non-geometric shot pattern to said laser device, wherein the non-geometric shaped shot pattern comprises an essentially straight section.
17. The method of claim 16 wherein the IOL is an FDA approved accommodating IOL.
18. The method of claim 16 wherein the IOL is an FDA approved IOL for near, intermediate and distance vision.
19. The method of claim 16 wherein the IOL is an FDA approved IOL that reduces or eliminates the need for spectacles.
20. The method of claim 16, wherein the predetermined shot pattern comprises a second essentially straight section.
21. The method of claim 20, wherein the predetermined shot pattern comprises a first curved section and a second curved section.
22. The method of claim 21, wherein: the essentially straight section is connected to the first and second curved sections.
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Type: Grant
Filed: Jul 24, 2009
Date of Patent: Jul 9, 2013
Patent Publication Number: 20100022995
Assignee: LensAR, Inc. (Orlando, FL)
Inventors: Rudolph W. Frey (Maitland, FL), Gary P. Gray (Orlando, FL)
Primary Examiner: Darryl J Collins
Application Number: 12/509,412